The true toughness of human cortical bone measured with realistically short cracks.

Bone is more difficult to break than to split. Although this is well known, and many studies exist on the behaviour of long cracks in bone, there is a need for data on the orientation-dependent crack-growth resistance behaviour of human cortical bone that accurately assesses its toughness at appropriate size scales. Here, we use in situ mechanical testing to examine how physiologically pertinent short (<600 microm) cracks propagate in both the transverse and longitudinal orientations in cortical bone, using both crack-deflection/twist mechanics and nonlinear-elastic fracture mechanics to determine crack-resistance curves. We find that after only 500 microm of cracking, the driving force for crack propagation was more than five times higher in the transverse (breaking) direction than in the longitudinal (splitting) direction owing to major crack deflections/twists, principally at cement sheaths. Indeed, our results show that the true transverse toughness of cortical bone is far higher than previously reported. However, the toughness in the longitudinal orientation, where cracks tend to follow the cement lines, is quite low at these small crack sizes; it is only when cracks become several millimetres in length that bridging mechanisms can fully develop leading to the (larger-crack) toughnesses generally quoted for bone.

Measurement of the toughness of bone: a tutorial with special reference to small animal studies.

Quantitative assessment of the strength and toughness of bone has become an integral part of many biological and bioengineering studies on the structural properties of bone and their degradation due to aging, disease and therapeutic treatment. Whereas the biomechanical techniques for characterizing bone strength are well documented, few studies have focused on the theory, methodology, and various experimental procedures for evaluating the fracture toughness of bone, i.e., its resistance to fracture, with particular reference to whole bone testing in small animal studies. In this tutorial, we consider the many techniques for evaluating toughness and assess their specific relevance and application to the mechanical testing of small animal bones. Parallel experimental studies on wild-type rat and mouse femurs are used to evaluate the utility of these techniques and specifically to determine the coefficient of variation of the measured toughness values.

Effect of aging on the transverse toughness of human cortical bone: evaluation by R-curves.

The age-related deterioration in the quality (e.g., strength and fracture resistance) and quantity (e.g., bone-mineral density) of human bone, together with increased life expectancy, is responsible for increasing incidence of bone fracture in the elderly. The present study describes ex vivo fracture experiments to quantitatively assess the effect of aging on the fracture toughness properties of human cortical bone specifically in the transverse (breaking) orientation. Because bone exhibits rising crack-growth resistance with crack extension, the aging-related transverse toughness is evaluated in terms of resistance-curve (R-curve) behavior, measured for bone taken from a wide range of age groups (25-74 years). Using this approach, both the ex vivo crack-initiation and crack-growth toughness are determined and are found to deteriorate with age; however, the effect is far smaller than that reported for the longitudinal toughness of cortical bone. Whereas the longitudinal crack-growth toughness has been reported to be reduced by almost an order of magnitude for human cortical bone over this age range, the corresponding age-related decrease in transverse toughness is merely ~14%. Similar to that reported for X-ray irradiated bone, with aging cracks in the transverse direction are subjected to an increasing incidence of crack deflection, principally along the cement lines, but the deflections are smaller and result in a generally less tortuous crack path.

Indentation techniques for evaluating the fracture toughness of biomaterials and hard tissues.

Indentation techniques for assessing fracture toughness are attractive due to the simplicity and expediency of experiments, and because they potentially allow the characterization of both local and bulk fracture properties. Unfortunately, rarely have such techniques been proven to give accurate fracture toughness values. This is a concern, as such techniques are seeing increasing usage in the study of biomaterials and biological hard tissues. Four available indentation techniques are considered in the present article: the Vickers indentation fracture (VIF) test, the cube corner indentation fracture (CCIF) test, the Vickers crack opening displacement (VCOD) test and the interface indentation fracture (IIF) test. Each technique is discussed in terms of its suitability for assessing the absolute and relative toughness of materials or material interfaces based on the published literature on the topic. In general, the VIF and CCIF techniques are found to be poor for quantitatively evaluating toughness of any brittle material, and the large errors involved (approximately +/-50%) make their applicability as comparative techniques limited. Indeed, indentation toughness values must differ by at least by a factor of three to conclude a significant difference in actual toughness. Additionally, new experimental results are presented on using the CCIF test to evaluate the fracture resistance of human cortical bone. Those new results indicate that inducing cracking is difficult, and that the cracks that do form are embedded in the plastic zone of the indent, invalidating the use of linear elastic fracture mechanics based techniques for evaluating the toughness associated with those cracks. The VCOD test appears to be a good quantitative method for some glasses, but initial results suggest there may be problems associated with applying this technique to other brittle materials. Finally, the IIF technique should only be considered a comparative or semi-quantitative technique for comparing material interfaces and/or the neighboring materials.